A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892066



Internal ID19186462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92710759..92731901hg38UCSC Ensembl
Outerchr11:92710759..92731901hg38UCSC Ensembl
Innerchr11:92443925..92465067hg19UCSC Ensembl
Outerchr11:92443925..92465067hg19UCSC Ensembl
Innerchr11:92083573..92104715hg18UCSC Ensembl
Outerchr11:92083573..92104715hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3821143
hg1921143
hg1821143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801401, essv25798209
Samples
Known GenesFAT3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892066
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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